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Quickie 2

FDA UDI

Class I (US FDA UDI)

by Sunrise Medical (US) LLC

Identity

Trade Name
Quickie 2 FDA UDI
Generic Name
Push-rim manual wheelchair, non-bariatric FDA UDI
Device Name
The Quickie 2 Family of chairs are folding ultra lightweight manual wheelchairs that offer strong frames without sacrificing weight savings. FDA UDI
Model / Reference
Quickie 2, Quickie 2 Lite, Quickie 2 Lite 2.0 FDA UDI
Description
The Quickie 2 Family of chairs are folding ultra lightweight manual wheelchairs that offer strong frames without sacrificing weight savings. FDA UDI

Identifiers

Catalog Number
EIQ2X FDA UDI
Primary DI / UDI-DI
00016958043815 FDA UDI
FDA Product Code
IOR FDA UDI
GMDN Term
Push-rim manual wheelchair, non-bariatric FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.3850 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Push-rim manual wheelchair, non-bariatric

Quickie 2 by Sunrise Medical (US) LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Push-rim manual wheelchair, non-bariatric.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 84b4dbd0-6704-49a4-a5af-d289f0cdc2e0 34 fields · synced Jun 9, 2026